Cure 360: MECP2 Reactivation | Interview with Toni Bedalov, MD, PhD | Rett Syndrome Research Trust

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  • čas přidán 22. 08. 2022
  • Toni Bedalov, MD, PhD, is one of several scientists collaborating on an MECP2 reactivation approach to cure Rett syndrome, which aims to awaken the healthy and silenced MECP2 gene in every girl with Rett. In collaboration with the labs of Kyle Fink, PhD, and Shawn Liu, PhD, Dr. Bedalov is using epigenome editing to achieve reactivation. Learn more in this short interview about current technologies and promising discoveries related to MECP2 reactivation that make Dr. Bedalov so hopeful about this genetic-based strategy for a Rett syndrome cure.
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    The Rett Syndrome Research Trust is singularly focused on a cure for Rett syndrome and related MECP2 disorders. Achieving success takes a deep understanding of the relevant science, an environment built for scientific collaboration, and experience with drug and business development. Today we are building on incredible scientific and industry momentum by implementing six genetic-based strategies that tackle Rett from every angle. Every single company pursuing a cure for Rett is able to do so because they leveraged discoveries and resources that were generated with RSRT funding. RSRT is the home of the Rett cure community, and we are confident that together we will cure Rett syndrome.

Komentáře • 5

  • @jennystuart-hill2756
    @jennystuart-hill2756 Před rokem

    Thank you for your ongoing dedication and hard work. I pray every day for a cure for Rett for all the children out there .

  • @teresadeneen3033
    @teresadeneen3033 Před rokem

    Thank you thank you and thank you for your hard work!

  • @michelemangora9240
    @michelemangora9240 Před rokem

    3 days ago Rett Syndrome MECP2 has been diagnosticated to my 3 years and 6 months old DAUGHTER

  • @sergiomorales2875
    @sergiomorales2875 Před rokem +1

    Is any of this available in the US? Are there any trials I will like to sign up my daughter

  • @melissarenteria4428
    @melissarenteria4428 Před rokem +1

    Have we tried something like bone marrow transplant. Or stem cells from a sibling compatible with the DNA of the child with Rett syndrome? Isn’t it possible for stem cells from embryo to produce normal copies of silenced MECP2 in our Rett children?